Clearance Summary
EMG - ESSENTIAL GAS MODULE, MODEL M1013A received FDA 510(k) clearance under submission number K041956, sponsored by Draeget Medical AG & Co. Kgaa. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2004-08-09.
- Submission: K041956
- Applicant / Sponsor: Draeget Medical AG & Co. Kgaa
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 2004-08-09
Classification & Regulation
This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.